GARDP’s vision is to ensure infections are treatable for everyone, everywhere. GARDP works with partners to accelerate the development of and access to treatments for drug-resistant infections that pose the greatest threat to health.

GARDP’s Integrity Line is an online third-party platform that can be used for the anonymous reporting of misconduct by GARDP staff or anyone outside the organization in connection with GARDP activities.

The purpose of this Code is to ensure a clear, achievable and relevant standard of ethical conduct for our activities. GARDP is committed to the highest level of integrity to ensure trust and confidence in GARDP’s operations.

GARDP has always been committed to the highest possible standards of openness, transparency, honesty and accountability, and is determined to maintain a culture of transparency and an opposition to fraud and corruption.

The purpose of the Conflict of interest Policy is to contribute to stakeholders’ trust in GARDP’s operations and support integrity in decision-making.

GARDP wishes to set standards of behaviour that all GARDP Staff are required to adhere to, with the understanding that we wish to foster a diverse, inclusive and tolerant workplace, and to provide assistance to those who need help.

GARDP’s procurement policy combines strict principles with pragmatic approaches in selecting the appropriate vendors, especially when the choice of qualified suppliers is limited.

This Data Protection Policy defines the objectives set by GARDP for the protection of individuals whose personal data is collected or received by GARDP, stored, and used internally, or otherwise transferred externally, and the good practices that must be applied within GARDP to ensure the protection of the rights and freedoms of these individuals (data subjects).

GARDP aims to stimulate increased involvement of public and private sectors in R&D for antimicrobial resistance.

Scientific publications are a key part of GARDP’s work as it is through scientific publications that results from research funded, supported, sponsored and/or conducted by GARDP is primarily communicated externally.

This GARDP Quality Policy (“Quality Policy”) outlines the organisational framework and principles meant to ensure the quality of the Products and compliance with relevant and/or applicable quality and regulatory requirements from investigational product research and development (non-clinical, clinical, pharmaceutical) to the manufacture, distribution and supply of the Products (“Product Lifecycle”).